I've heard from colleagues in the (US) medical industry that there are guidelines from the likes of AAMI and ECRI but few real "requirements". My second-hand un

I've heard from colleagues in the (US) medical industry that there are guidelines from the likes of AAMI and ECRI but few real "requirements". My second-hand understanding is that it's largely dependent on how much leverage the end-users (doctors and nurses) have to dictate system requirements and how much leverage the hospital system has with respect to negotiating with suppliers. Ref: https://www.ecri.org/alarm-safety-handbook https://www.ecri.org/alarm-safety-handbook https://www.jointcommission.org/resources/patient-safety-topics/sentinel-event/sentinel-event-alert-newsletters/sentinel-event-alert-issue-50-medical-device-alarm-safety-in-hospitals/ https://www.jointcommission.org/resources/patient-safety-top...